Bibliographic Details
| Title: |
Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation. |
| Authors: |
Netravathi, Manjunath1, Kumari, Renu2, Kapoor, Saketh3, Dakle, Pushkar2, Dwivedi, Manish Kumar2, Roy, Sumitabho Deb4, Pandey, Paritosh5, Saini, Jitender6, Ramakrishna, Anil1, Navalli, Devaraddi1, Satishchandra, Parthasarathy1, Pal, Pramod Kumar1 pal.pramod@rediffmail.com, Kumar, Arun3 karun@mrdg.jisc.ernet.in, Faruq, Mohammed2 faruq.mohd@igib.res.in |
| Source: |
BMC Medical Genetics. 2015, Vol. 16 Issue 1, p1-8. 8p. |
| Database: |
Academic Search Ultimate |
